Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
G |
A |
6: 128,522,030 (GRCm39) |
T1264I |
probably damaging |
Het |
Aadac |
T |
A |
3: 59,946,986 (GRCm39) |
V228E |
probably benign |
Het |
Abca4 |
A |
T |
3: 121,931,274 (GRCm39) |
R1436W |
probably benign |
Het |
Abo |
A |
G |
2: 26,738,287 (GRCm39) |
L39S |
probably benign |
Het |
Acnat1 |
T |
A |
4: 49,447,773 (GRCm39) |
R269S |
probably benign |
Het |
Adap2 |
T |
C |
11: 80,045,942 (GRCm39) |
V74A |
probably damaging |
Het |
Ahctf1 |
C |
A |
1: 179,603,638 (GRCm39) |
A803S |
possibly damaging |
Het |
Ak6 |
A |
G |
13: 100,792,003 (GRCm39) |
S149G |
probably benign |
Het |
Ank |
T |
C |
15: 27,591,588 (GRCm39) |
V444A |
probably damaging |
Het |
Armt1 |
AC |
A |
10: 4,400,848 (GRCm39) |
|
probably null |
Het |
Atf7 |
A |
C |
15: 102,462,286 (GRCm39) |
V112G |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,464,982 (GRCm39) |
Y1582C |
probably damaging |
Het |
Bricd5 |
G |
T |
17: 24,693,083 (GRCm39) |
|
probably benign |
Het |
Bsn |
C |
A |
9: 108,016,652 (GRCm39) |
E120* |
probably null |
Het |
Cacna1g |
T |
G |
11: 94,321,050 (GRCm39) |
N1348T |
probably damaging |
Het |
Ccnc |
T |
G |
4: 21,746,776 (GRCm39) |
|
probably null |
Het |
Cd163 |
A |
G |
6: 124,297,497 (GRCm39) |
D881G |
probably benign |
Het |
Cep295 |
G |
A |
9: 15,244,619 (GRCm39) |
P1279L |
probably benign |
Het |
Cic |
G |
A |
7: 24,971,414 (GRCm39) |
V382I |
possibly damaging |
Het |
Cyp21a1 |
G |
A |
17: 35,020,860 (GRCm39) |
S453F |
probably damaging |
Het |
D16Ertd472e |
A |
T |
16: 78,344,646 (GRCm39) |
I154N |
probably benign |
Het |
Dbf4 |
A |
G |
5: 8,447,764 (GRCm39) |
V482A |
possibly damaging |
Het |
Dchs2 |
G |
A |
3: 83,192,573 (GRCm39) |
V1673M |
probably benign |
Het |
Dctd |
T |
A |
8: 48,590,385 (GRCm39) |
C119S |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,717,065 (GRCm39) |
T1234A |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,621,255 (GRCm39) |
|
probably null |
Het |
Eya4 |
A |
T |
10: 22,999,805 (GRCm39) |
M386K |
|
Het |
Fbxw19 |
T |
A |
9: 109,315,101 (GRCm39) |
M154L |
probably benign |
Het |
Frmpd1 |
T |
A |
4: 45,279,182 (GRCm39) |
S636T |
probably benign |
Het |
Glb1l |
A |
T |
1: 75,177,683 (GRCm39) |
Y412N |
probably damaging |
Het |
Gnb5 |
T |
A |
9: 75,218,696 (GRCm39) |
L7Q |
probably damaging |
Het |
Gpr19 |
C |
T |
6: 134,864,704 (GRCm39) |
V3M |
unknown |
Het |
Hivep2 |
A |
G |
10: 14,007,505 (GRCm39) |
T1368A |
probably damaging |
Het |
Hmx3 |
A |
T |
7: 131,146,102 (GRCm39) |
Q270L |
probably damaging |
Het |
Il1rap |
A |
T |
16: 26,533,675 (GRCm39) |
I524F |
possibly damaging |
Het |
Mettl17 |
G |
A |
14: 52,125,491 (GRCm39) |
G198D |
probably damaging |
Het |
Mga |
T |
A |
2: 119,765,999 (GRCm39) |
I1421N |
possibly damaging |
Het |
Myb |
T |
A |
10: 21,026,275 (GRCm39) |
Q231L |
probably benign |
Het |
Myef2l |
T |
A |
3: 10,154,407 (GRCm39) |
M392K |
probably benign |
Het |
Myf5 |
G |
A |
10: 107,321,527 (GRCm39) |
T89I |
probably damaging |
Het |
Nup214 |
T |
A |
2: 31,937,523 (GRCm39) |
L1999Q |
probably damaging |
Het |
Or10aa3 |
T |
C |
1: 173,878,329 (GRCm39) |
L130P |
|
Het |
Or1ad6 |
T |
A |
11: 50,860,613 (GRCm39) |
L256Q |
probably damaging |
Het |
Or4a76 |
A |
G |
2: 89,460,388 (GRCm39) |
Y285H |
probably damaging |
Het |
Or51t4 |
A |
T |
7: 102,598,443 (GRCm39) |
H257L |
probably damaging |
Het |
Or5w19 |
G |
A |
2: 87,698,379 (GRCm39) |
G15R |
probably damaging |
Het |
Or7a36 |
A |
G |
10: 78,820,220 (GRCm39) |
M199V |
probably benign |
Het |
Otog |
A |
T |
7: 45,916,721 (GRCm39) |
D886V |
possibly damaging |
Het |
Pigs |
T |
C |
11: 78,230,213 (GRCm39) |
Y327H |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,563,383 (GRCm39) |
V478A |
probably damaging |
Het |
Pnrc1 |
C |
A |
4: 33,246,488 (GRCm39) |
G157V |
probably damaging |
Het |
Poglut1 |
G |
T |
16: 38,347,137 (GRCm39) |
S343R |
probably benign |
Het |
Ppwd1 |
A |
G |
13: 104,346,155 (GRCm39) |
M500T |
possibly damaging |
Het |
Pyy |
C |
T |
11: 101,998,111 (GRCm39) |
G23E |
probably damaging |
Het |
Ripor3 |
T |
A |
2: 167,831,238 (GRCm39) |
D521V |
probably benign |
Het |
Rnpepl1 |
T |
C |
1: 92,845,424 (GRCm39) |
S448P |
probably benign |
Het |
Sash1 |
G |
A |
10: 8,637,994 (GRCm39) |
|
probably benign |
Het |
Sbf2 |
T |
C |
7: 110,040,702 (GRCm39) |
Q375R |
possibly damaging |
Het |
Synj1 |
C |
T |
16: 90,741,740 (GRCm39) |
C1252Y |
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,960,246 (GRCm39) |
L1027Q |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,637 (GRCm39) |
V1796A |
possibly damaging |
Het |
Timp3 |
A |
T |
10: 86,136,782 (GRCm39) |
E22V |
possibly damaging |
Het |
Tlk1 |
A |
C |
2: 70,617,219 (GRCm39) |
|
probably null |
Het |
Tmco1 |
C |
A |
1: 167,141,700 (GRCm39) |
T69K |
|
Het |
Topaz1 |
T |
A |
9: 122,626,728 (GRCm39) |
M1452K |
probably benign |
Het |
Tsc22d2 |
T |
C |
3: 58,367,453 (GRCm39) |
Y668H |
unknown |
Het |
Uri1 |
A |
T |
7: 37,669,031 (GRCm39) |
D153E |
probably benign |
Het |
Vmn1r169 |
A |
T |
7: 23,277,342 (GRCm39) |
T245S |
probably damaging |
Het |
Vmn1r60 |
A |
G |
7: 5,547,918 (GRCm39) |
Y61H |
|
Het |
Zfp541 |
A |
T |
7: 15,806,139 (GRCm39) |
E91D |
probably damaging |
Het |
Zfp946 |
A |
G |
17: 22,673,569 (GRCm39) |
N108D |
possibly damaging |
Het |
Zpr1 |
T |
C |
9: 46,186,747 (GRCm39) |
L194P |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,755,653 (GRCm39) |
N1027K |
possibly damaging |
Het |
|
Other mutations in Pde7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01349:Pde7a
|
APN |
3 |
19,283,843 (GRCm39) |
unclassified |
probably benign |
|
IGL02644:Pde7a
|
APN |
3 |
19,311,031 (GRCm39) |
splice site |
probably benign |
|
IGL02968:Pde7a
|
APN |
3 |
19,297,285 (GRCm39) |
nonsense |
probably null |
|
IGL02985:Pde7a
|
APN |
3 |
19,365,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Pde7a
|
UTSW |
3 |
19,295,697 (GRCm39) |
splice site |
probably benign |
|
R0736:Pde7a
|
UTSW |
3 |
19,285,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R0834:Pde7a
|
UTSW |
3 |
19,284,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Pde7a
|
UTSW |
3 |
19,314,408 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1955:Pde7a
|
UTSW |
3 |
19,281,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R2943:Pde7a
|
UTSW |
3 |
19,284,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4072:Pde7a
|
UTSW |
3 |
19,311,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R4366:Pde7a
|
UTSW |
3 |
19,365,026 (GRCm39) |
critical splice donor site |
probably null |
|
R4524:Pde7a
|
UTSW |
3 |
19,285,140 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4666:Pde7a
|
UTSW |
3 |
19,314,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R4698:Pde7a
|
UTSW |
3 |
19,365,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R4850:Pde7a
|
UTSW |
3 |
19,297,281 (GRCm39) |
missense |
probably benign |
|
R4859:Pde7a
|
UTSW |
3 |
19,295,655 (GRCm39) |
intron |
probably benign |
|
R5283:Pde7a
|
UTSW |
3 |
19,314,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Pde7a
|
UTSW |
3 |
19,287,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R5702:Pde7a
|
UTSW |
3 |
19,295,371 (GRCm39) |
nonsense |
probably null |
|
R5756:Pde7a
|
UTSW |
3 |
19,319,009 (GRCm39) |
missense |
probably benign |
0.08 |
R5784:Pde7a
|
UTSW |
3 |
19,319,009 (GRCm39) |
missense |
probably benign |
0.08 |
R6301:Pde7a
|
UTSW |
3 |
19,297,327 (GRCm39) |
missense |
probably benign |
0.01 |
R7136:Pde7a
|
UTSW |
3 |
19,285,258 (GRCm39) |
missense |
probably benign |
0.36 |
R7291:Pde7a
|
UTSW |
3 |
19,281,838 (GRCm39) |
missense |
probably benign |
|
R7685:Pde7a
|
UTSW |
3 |
19,281,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8032:Pde7a
|
UTSW |
3 |
19,314,429 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8884:Pde7a
|
UTSW |
3 |
19,281,858 (GRCm39) |
missense |
probably benign |
|
R9648:Pde7a
|
UTSW |
3 |
19,310,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Pde7a
|
UTSW |
3 |
19,285,167 (GRCm39) |
missense |
probably benign |
0.01 |
|